Clinical Regulatory Writer (US or Canada)

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Do you have a flair for Clinical Regulatory Writing?

If you love writing, have a passion for clinical regulatory strategy, have experience with biologics, and are looking for an opportunity that will allow you to continue to have the flexibility of working from home while gaining tremendous professional experience and working with some of the Industry’s BEST, then Parexel's Regulatory Consulting team has an amazing opportunity for you!

As a Clinical Regulatory Writer, you will:

Be responsible for Regulatory technical writing (clinically focused) to support development of clinical documents in accordance with ICH/E6/GCP guidelines to support US submissions, clinical trial applications, and clinical consultation responses for multiple clients.

Qualifications:

• RA professional with 4+ yrs experience in clinical development that includes writing of clinical technical documents and a strong understanding of ICH/E6/GCP guidelines.

  • Primarily seeking an experienced Clinical author to support FDA submissions:

    • New INDs

    • Pediatric Plans, Fast Track Applications, Breakthrough Therapy Applications, Orphan Drug Applications, responses to FDA requests, Meeting Request and Packages

    • NDA/BLA submissions

• Ability to interpret data and advice from regulatory authorities objectively, often in the face of strongly held competing views.

• Extensive experience of all phases of the drug development process in regulatory affairs, including projects with little or no precedence.

• Extensive knowledge of being able to develop product/therapeutic knowledge in a new area.

• Previous experience independently authoring clinical modules for FDA submissions is required. EU submissions experience is a plus.

• Previous Biologics experience is required. Previous device experience is a plus.

• Previous experience with oncology or rare disease products is a plus.

• Previous nonclinical regulatory writing experience is a plus.

• Bachelor’s, Master’s or PhD in science/biological or healthcare.

EEO Disclaimer
Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.